Devices

Device Recall Maquet Cardiopulmonary Bypass Custom Tubing kit

Model / Serial
Batch Number 3000018640, UDI Code 10607567205373; Batch Number 3000020516, UDI Code 10607567205373
Product Classification
Cardiovascular Devices
Device Class
2
Implanted device?
No
Distribution
The products were distributed to the following US states: AL, OR, and TX.
Product Description
Maquet Cardiopulmonary Bypass Custom Tubing kit BEQ-TOP 5909 14 Pack QPID, Part Number 701064992
Manufacturer
Datascope Corporation
1 Event
- Recall of Device Recall Maquet Cardiopulmonary Bypass Custom Tubing kit

Manufacturer

Datascope Corporation

Manufacturer Address
Datascope Corporation, 15 Law Dr, Fairfield NJ 07004-3206
Manufacturer Parent Company (2017)
Getinge AB
Source
USFDA

One device with a similar name

Learn more about the data here

Device Recall Maquet Cardiopulmonary Bypass Custom Tubing kit

Model / Serial
Batch Number 3000020957, UDI Code 10607567203522
Product Classification
Cardiovascular Devices
Device Class
2
Implanted device?
No
Distribution
The products were distributed to the following US states: AL, OR, and TX.
Product Description
Maquet Cardiopulmonary Bypass Custom Tubing kit BEQ-TOP 15801 Neonatal Special, Part Number 701055490
Manufacturer
Datascope Corporation

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Medical devices help to diagnose, prevent and treat many injuries and diseases. We are not suggesting or implying that any companies or other entities included in the International Medical Devices Database engaged in unlawful conduct or otherwise acted improperly. The same device may have different names in different countries. This database is not intended to provide medical advice and patients should check with their doctors to determine if it contains relevant information and if such information has medical implications for them.

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